Last synced on 23 September 2022 at 11:05 pm

Reperen Surgical Mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170134
510(k) Type
Traditional
Applicant
IconLab Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2017
Days to Decision
204 days
Submission Type
Summary

Reperen Surgical Mesh

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K170134
510(k) Type
Traditional
Applicant
IconLab Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/9/2017
Days to Decision
204 days
Submission Type
Summary